#

Quality Compliance Associate

SIRE Life Sciences®

Netherlands, zagranica

SIRE Life Sciences®

Quality Compliance Associate

Location: Netherlands

SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!

THE COMPANY

Our client is a professional Pharmaceutical organization, based in Noord-Holland Netherlands.

They are one of the big players in the Dutch pharmaceutical industry, pioneering innovative concepts. They offer opportunity for own initiative concerning improvement and expansion of their quality management systems.

ROLE DESCRIPTION

You will be taking the department to a whole other level with regards to compliance. Together with your colleagues you will ensure continuous improvement and you in particular will be responsible for writing reviews, both for annual reports as for product quality, so that all the regulatory guidelines are met.

RESPONSIBILITIES

- Writing reports and GMP procedures
- Reviewing annual and product quality reports and indicating possible deviations and points of improvement
- Executing trend analyses
- Scrutinize current audits and regulations while transiting improvements to the QMS

REQUIREMENTS

- BSc. in life science related field
- Minimum of 3 years of experience in a pharmaceutical environment
- Experience with writing reports, reviews and GMP documentation
- Knowledge of GxP guidelines is preferred
- Experience with project management is preferred
- Fluent in Dutch and English

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Amber Moet.

Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
SIRE Life Sciences®

Czy chcesz otrzymywać oferty pracy na podobne stanowiska?

Utwórz powiadomienie e-mail
Zapisz mnie

Zapisani kandydaci otrzymują informacje jako pierwsi.

Podziel się ze znajomymi